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Autoimmune encephalitis mediated by antibodies against the n-methyl-d-aspartate receptor: Report of four cases in Peru

Original title: Encefalitis autoinmune mediada por anticuerpos contra el receptor n-metil-d-aspartato: Reporte de cuatro casos en Perú
  • Henry Palomino-Lescano(corresponding author)
    ,
  • Darwin Segura-Chávez
    ,
  • Darko Quispe-Orozco
    ,
  • ,
  • Walter De la Cruz
    ,
  • Willy Zapata-Luyo
*Corresponding author for this work
  • docencia y atención especializada en epilepsia
    ,
  • ,
  • CBI en Demencias y Enfermedades Desmielinizantes del Sistema Nervioso
    ,
  • Hospital Hipólito Unanue de Tacna
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

Spanish

Pages from-to (Number of pages)

Pages 138-144 (7 pages)

Journal (Volume, Issue Number)

Revista peruana de medicina experimental y salud publica (Volume 36, Issue 1)

Publication milestones

  • Published - 03/2019

Publication status

Published - 03/2019

ISSN

1726-4634

Publication IDs

  • Scopus: 85066479634
  • PubMed: 31116328

Abstract

Autoimmune encephalitis with antibodies against the N-methyl-D-aspartate receptor (anti-NMDAR) is a disorder mediated by antibodies against neural surface antigens, whose early diagnosis and timely treatment improve the prognosis of the disease. Four cases with the definitive diagnosis of autoimmune encephalitis by anti-NMDAR are presented, treated at the National Institute of Neurological Sciences in Lima-Peru. All patients had epileptic seizures and three cases developed a refractory epileptic state. In addition, three patients presented neuropsychiatric alterations, dyskinesias, and dysautonomia. Two cases required ventilatory support. All presented an abnormal electroencephalogram; two cases had pleocytosis in cerebrospinal fluid, and only one showed brain abnormalities on MRI. Regarding treatment, all patients received methylprednisolone immunotherapy and only two of them required plasma exchange for an ineffective response to corticosteroid treatment. After 12 months of hospital discharge, three patients were free of epileptic seizures and only one case did not achieve functional independence. These cases show that anti-NMDAR encephalitis is a treatable condition and its early recognition together with appropriate treatment (immunotherapy/plasmapheresis) are essential for a favorable evolution.

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